Cas 144405-58-3,(+/-)-3-benzyl-1-(2'α,3'α-dihydroxy-4'β-hydroxymethylcyclopent-1'β-yl)-2,4(1H,3H)-pyrimidinedione

144405-58-3

Post Buying Request

Basic information

Product Name: (+/-)-3-benzyl-1-(2'α,3'α-dihydroxy-4'β-hydroxymethylcyclopent-1'β-yl)-2,4(1H,3H)-pyrimidinedione
Synonyms:
CAS NO:144405-58-3
Molecular Formula:
Molecular Weight: 332.356
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (+/-)-3-benzyl-1-(2'α,3'α-dihydroxy-4'β-hydroxymethylcyclopent-1'β-yl)-2,4(1H,3H)-pyrimidinedione(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-3-benzyl-1-(2'α,3'α-dihydroxy-4'β-hydroxymethylcyclopent-1'β-yl)-2,4(1H,3H)-pyrimidinedione(144405-58-3)
EPA Substance Registry System: (+/-)-3-benzyl-1-(2'α,3'α-dihydroxy-4'β-hydroxymethylcyclopent-1'β-yl)-2,4(1H,3H)-pyrimidinedione(144405-58-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 144405-58-3(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

144405-58-3 Suppliers

Recommended suppliers

144405-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144405-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,0 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144405-58:
(8*1)+(7*4)+(6*4)+(5*4)+(4*0)+(3*5)+(2*5)+(1*8)=113
113 % 10 = 3
So 144405-58-3 is a valid CAS Registry Number.

144405-58-3Upstream product

144405-58-3Downstream Products

144405-58-3Relevant academic research and scientific papers

Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams

Katagiri,Muto,Nomura,Higashikawa,Kaneko

, p. 1112 - 1122 (2007/10/02)

Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 144405-58-3